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MiMo(TM) Negative Pressure Wound Therapy System

Page Type
Cleared 510(K)
510(k) Number
K181929
510(k) Type
Traditional
Applicant
Baymax Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2019
Days to Decision
252 days
Submission Type
Summary

MiMo(TM) Negative Pressure Wound Therapy System

Page Type
Cleared 510(K)
510(k) Number
K181929
510(k) Type
Traditional
Applicant
Baymax Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2019
Days to Decision
252 days
Submission Type
Summary